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Planning Actions for Consistent Engagement

Manipulating Action Plans to Improve Physical Activity Behavior and Cognitive Health in Older Adults

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07447401
Acronym
PACE
Enrollment
148
Registered
2026-03-03
Start date
2027-01-01
Completion date
2028-07-01
Last updated
2026-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognition, Habits, Physical Activity

Keywords

Action Planning, Physical Activity, Cognition, Habit, Older Adults

Brief summary

The goal of this clinical trial is to evaluate whether different approaches to action planning can promote physical activity (PA) habits, increase PA behavior, and improve cognitive functioning in older adults who are currently inactive or insufficiently active. The main questions it aims to answer are: 1. Does a trial-and-error approach to PA action planning lead to greater improvements in PA habits, PA behavior, and cognitive functioning compared to standard PA planning or non-PA planning? 2. Does greater consistency and successful enactment of action plans result in more substantial changes in PA habits, behavior, and cognitive functioning? Researchers will compare three groups to determine which planning approach yields superior outcomes.: 1. Non-PA planning (generic weekly planning) 2. PA planning (weekly planning for PA) 3. PA trial-and-error planning (weekly PA plans followed by preferred plan adoption) Participants will: 1. Wear Fitbit monitors continuously for 9 months to track PA behavior 2. Complete mobile cognitive assessments daily for 7 days before the intervention, monthly during the intervention, and at follow-up 3. Create action plans and report on PA habits, intentions, and plan enactment weekly during the intervention and at follow-up

Interventions

BEHAVIORALNon-PA Action Planning

Participants will create weekly action plans to engage in one of four non-PA health behaviors (i.e., practice good sleep hygiene, make healthy food choices, wash my hands, practice good oral hygiene). Action plans will include specifying when, where, how, with whom participants will engage in the target behavior over the upcoming week.

BEHAVIORALPA Action Planning

Participants will create weekly action plans to engage in physical activity. Action plans will include specifying when, where, how, with whom participants will engage in physical activity over the upcoming week.

BEHAVIORALConsistency in Action Plans

Participants will be given six weeks to experiment with different physical activity action plans (changing the contextual features of the plan). In the seventh week, participants will be encouraged to stick with their best plan for the remaining weeks of the intervention. By maintaining the same plan over the remaining weeks of the intervention, this should promote context stability of the planned behavior.

Sponsors

University of North Carolina, Greensboro
Lead SponsorOTHER
University of South Carolina
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* age 60 years or older * own a smartphone * willingness to download an app onto their personal smartphone and complete the cognitive assessments and questionnaires on their smartphone, wear the accelerometer, and undergo randomization * insufficient PA (i.e., not meeting current PA guidelines) but report intentions to increase their PA over the next 6 months * self-reported ability to ambulate without assistance * English as a primary language

Exclusion criteria

* Individuals that are unwilling or unable to obtain medical clearance (if needed) * have received a diagnosis of mild cognitive impairment or ADRD * concurrently participating in another study involving PA or weight loss * planning to have surgery or relocate within the next 9 months

Design outcomes

Primary

MeasureTime frameDescription
Change in Device-Based Physical Activity from Baseline to 6 MonthsDevice-based physical activity will be assessed daily during the 7-day baseline, daily during the 6-month intervention, and daily during the 3-month follow-up period.The wrist-worn Fitbit Inspire will provide an device-based measure of minutes/day of moderate-to-vigorous physical activity (based on step cadence)

Secondary

MeasureTime frameDescription
Change in Grid Memory Task Performance from Baseline to 6 MonthsThe Grid Memory Task will be administered for 7 consecutive days at baseline, for 7 days each month during the 6 month intervention, and for 7 days at the end of the 3-month follow-up.The Grid Memory Task from the Mobile Monitoring of Cognitive Change Toolkit will be administered through participants' smartphone for 7 consecutive days (with morning and evening assessments) at each timepoint and measures working memory. The primary outcome for Grid Memory Task is the Euclidean distance of the red dots between study and recall arrays.
Change in Symbol Search Task Performance from Baseline to 6 MonthsThe Search Symbol Task will be administered for 7 consecutive days at baseline, for 7 days each month during the 6 month intervention, and for 7 days at the end of the 3-month follow-up.The Search Symbol Task from the Mobile Monitoring of Cognitive Change Toolkit will be administered through participants' smartphone for 7 consecutive days (with morning and evening assessments) at each timepoint and measures processing speed. The primary outcome of Search Symbol Task is the median response time for accurate trials.
Change in Physical Activity Habit Strength from Baseline to 6 MonthsThe single item will be administered baseline, weekly during the 6-month intervention, and at the end of the 3-month follow-up.A single item from the Self-Reported Behavioural Automaticity Index (i.e., "Being physically active is something I do automatically.") will be administered weekly on participants' smartphone and measures physical activity habit strength. Participants will respond on a 7-point Likert scale with higher values indicating stronger habit strength.

Countries

United States

Contacts

CONTACTJaclyn Maher
jpmaher@uncg.edu336-256-1379

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026